The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125360002 12536000 2 F 20160606 20160707 20160707 EXP US-CIPLA LTD.-2016US06769 CIPLA 0.00 Y 0.00000 20160707 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125360002 12536000 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, QD 77073 5 MG TABLET
125360002 12536000 2 C PREDNISONE. PREDNISONE 1 Unknown 5 MG, QD U U 0 5 MG
125360002 12536000 3 C METHOTREXATE. METHOTREXATE 1 Unknown 2.5 MG, QD U U 0 2.5 MG
125360002 12536000 4 C PREVACID LANSOPRAZOLE 1 Unknown 30 MG, QD U U 0 30 MG CAPSULE
125360002 12536000 5 C DIOVAN VALSARTAN 1 Unknown 320 MG, QD U U 0 320 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125360002 12536000 1 Hypertension
125360002 12536000 2 Rheumatoid arthritis
125360002 12536000 3 Rheumatoid arthritis
125360002 12536000 4 Hyperchlorhydria
125360002 12536000 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125360002 12536000 Abdominal pain upper
125360002 12536000 Feeling abnormal
125360002 12536000 Headache
125360002 12536000 Hunger
125360002 12536000 Nausea
125360002 12536000 Rash generalised
125360002 12536000 Skin disorder
125360002 12536000 Somnolence

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found